@article { ISI:000287801700007,
	title = {Synthetic studies of superstolide A: a carbohydrate based synthesis of the C21-C26 segment},
	journal = {Letters in Organic Chemistry},
	volume = {7},
	number = {8},
	year = {2010},
	month = {DEC},
	pages = {657-660},
	publisher = {BENTHAM SCIENCE PUBL LTD},
	address = {EXECUTIVE STE Y26, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATES},
	abstract = {<p>The synthesis of C21-C26 fragment of superstolide A, starting from D-glucose diacetonide, involving regioselective ring opening of epoxide by Grignard reagent and regioselective stereospecefic hydroboration oxidation has been described.</p>},
	keywords = {Chiral pool, Potent cytotoxic, Regioselective epoxide opening, Stereoselective hydroboration-oxidation, Superstolide A},
	issn = {1570-1786},
	doi = {10.2174/157017810793811704},
	author = {Pal, Rita and Rahaman, Hasibur and Mohapatra, Debendra K. and Gurjar, Mukund K.}
}
